Condition: Acute Myeloid Leukemia · Sponsor: Imbioray (Hangzhou) Biomedicine Co., Ltd.
This is an open-label clinical study: phase Ia is the dose-escalation part, and phase Ib is the dose-expansion part. The phase Ia study is to evaluate the safety, tolerability, recommended phase II dose, pharmacokinetics, immunogenicity and preliminary efficacy of IBR733 cell injection in relapsed/refractory acute myeloid leukemia (AML).
This description comes directly from the study's public registry record.
Depei Wu, MD, PhD · 67781856 · wudepei@suda.edu.cn
Xiaowen Tang, MD, PhD · 67781856 · tangxiaowen@suda.edu.cn
Always discuss trial participation with your own doctor first.
| The First Affiliated Hospital of Soochow University | Suzhou, Jiangsu, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06234904